Regular Strength Pain Relief

Product NDC: 70518-3253
11-digit product format: 705183253
Labeler code: 70518
Product ID: 70518-3253_cf2df306-de38-c141-e053-2a95a90a4d74
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen
Dosage form: TABLET
Route: ORAL
Labeler: REMEDYREPACK INC.
Application: part343
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2021-10-22
Marketing end: 0000-00-00
Substance: ACETAMINOPHEN
Active strength: 325 mg/1
NDC exclude flag: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70518-3253-0	2023-10-12	C162847	48780-1	f386c649-9a65-0266-e053-dadaa90a7c1a	2b992a1b-4838-4699-b4f2-a4f9774fd809
70518-3253-0	2023-01-30	C162847	48780-1	f386c649-9a65-0266-e053-dadaa90a7c1a	2b992a1b-4838-4699-b4f2-a4f9774fd809

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
70518-3253-0	EA - Each	70518-3253	bc507f11-b7ad-41d0-8fae-0bcb885b0284	1	2023-01-09

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
70518-3253-0	70518325300	20 TABLET in 1 BLISTER PACK (70518-3253-0)	20 tablet	2021-10-22	0000-00-00	No	No	Current